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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:RAD51C-RPIA (FusionGDB2 ID:71318)

Fusion Gene Summary for RAD51C-RPIA

check button Fusion gene summary
Fusion gene informationFusion gene name: RAD51C-RPIA
Fusion gene ID: 71318
HgeneTgene
Gene symbol

RAD51C

RPIA

Gene ID

5889

22934

Gene nameRAD51 paralog Cribose 5-phosphate isomerase A
SynonymsBROVCA3|FANCO|R51H3|RAD51L2RPI|RPIAD
Cytomap

17q22

2p11.2

Type of geneprotein-codingprotein-coding
DescriptionDNA repair protein RAD51 homolog 3RAD51-like protein 2yeast RAD51 homolog 3ribose-5-phosphate isomerasephosphoriboisomeraseribose 5-phosphate epimerase
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000583539, ENST00000337432, 
ENST00000487921, ENST00000421782, 
ENST00000283646, 
Fusion gene scores* DoF score3 X 3 X 3=274 X 3 X 3=36
# samples 34
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RAD51C [Title/Abstract] AND RPIA [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRAD51C(56770046)-RPIA(89028796), # samples:1
Anticipated loss of major functional domain due to fusion event.RAD51C-RPIA seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
RAD51C-RPIA seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
RAD51C-RPIA seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
RAD51C-RPIA seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneRAD51C

GO:0006281

DNA repair

19451272

HgeneRAD51C

GO:0006310

DNA recombination

19451272


check buttonFusion gene breakpoints across RAD51C (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across RPIA (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-CG-5721-01ARAD51Cchr17

56770046

+RPIAchr2

89028796

+


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Fusion Gene ORF analysis for RAD51C-RPIA

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000583539ENST00000283646RAD51Cchr17

56770046

+RPIAchr2

89028796

+
Frame-shiftENST00000337432ENST00000283646RAD51Cchr17

56770046

+RPIAchr2

89028796

+
intron-3CDSENST00000487921ENST00000283646RAD51Cchr17

56770046

+RPIAchr2

89028796

+
Frame-shiftENST00000421782ENST00000283646RAD51Cchr17

56770046

+RPIAchr2

89028796

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for RAD51C-RPIA


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for RAD51C-RPIA


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for RAD51C-RPIA


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for RAD51C-RPIA


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for RAD51C-RPIA


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for RAD51C-RPIA


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRAD51CC0346153Breast Cancer, Familial7CLINGEN
HgeneRAD51CC3150653FANCONI ANEMIA, COMPLEMENTATION GROUP O6CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneRAD51CC3150659BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 35CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneRAD51CC0015625Fanconi Anemia4CTD_human;GENOMICS_ENGLAND
HgeneRAD51CC0006142Malignant neoplasm of breast2CTD_human
HgeneRAD51CC0677776Hereditary Breast and Ovarian Cancer Syndrome2ORPHANET
HgeneRAD51CC0678222Breast Carcinoma2CTD_human
HgeneRAD51CC1257931Mammary Neoplasms, Human2CTD_human
HgeneRAD51CC1458155Mammary Neoplasms2CTD_human
HgeneRAD51CC4704874Mammary Carcinoma, Human2CTD_human
HgeneRAD51CC0023465Acute monocytic leukemia1GENOMICS_ENGLAND
HgeneRAD51CC0023467Leukemia, Myelocytic, Acute1GENOMICS_ENGLAND
HgeneRAD51CC0030312Pancytopenia1GENOMICS_ENGLAND
HgeneRAD51CC0265219Miller Dieker syndrome1GENOMICS_ENGLAND
HgeneRAD51CC0919267ovarian neoplasm1CTD_human
HgeneRAD51CC1140680Malignant neoplasm of ovary1CTD_human;GENOMICS_ENGLAND
HgeneRAD51CC1855710Bone marrow hypocellularity1GENOMICS_ENGLAND
HgeneRAD51CC3463824MYELODYSPLASTIC SYNDROME1GENOMICS_ENGLAND
HgeneRAD51CC4228778Abnormality of radial ray1GENOMICS_ENGLAND
TgeneRPIAC1291609Ribose 5-Phosphate Isomerase Deficiency4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT